Primary Device ID | 00690103187267 |
NIH Device Record Key | 750b6a9d-fbfa-42e7-bb32-38c35c6366ec |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VIGILEO |
Version Model Number | MHFD1 |
Catalog Number | MHFD1 |
Company DUNS | 134139174 |
Company Name | Edwards Lifesciences LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)822-9637 |
tech_support@edwards.com | |
Phone | +1(800)822-9637 |
tech_support@edwards.com |
Length | 96 Inch |
Length | 96 Inch |
Special Storage Condition, Specify | Between 0 and 0 *STORE IN A COOL, DRY PLACE. |
Special Storage Condition, Specify | Between 0 and 0 *STORE IN A COOL, DRY PLACE. |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00690103187267 [Primary] |
DQE | CATHETER, OXIMETER, FIBEROPTIC |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-03 |
00690103187267 | VIGILEO ANALOG SLAVE CABLE, DATEX DIN7 |
00690103186093 | PRESSURE SLAVE CABLE |
00690103181456 | PRESSURE SLAVE CABLE |
00690103181449 | PRESSURE SLAVE CABLE |
00690103181418 | PRESSURE SLAVE CABLE |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
VIGILEO 78466015 3382745 Live/Registered |
Edwards Lifsciences Corporation 2004-08-11 |